APA (7th ed.) Citation

Chih-Ping Chen, Yi-Ning Su, Fang-Yu Hung, Schu-Rern Chern, Jun-Wei Su, & Wayseen Wang. (2012). Identification of a COL1A2 mutation with a deletion spanning coding and intronic sequence in exon 19 and intron 19 in a fetus with osteogenesis imperfecta type II. Elsevier.

Chicago Style (17th ed.) Citation

Chih-Ping Chen, Yi-Ning Su, Fang-Yu Hung, Schu-Rern Chern, Jun-Wei Su, and Wayseen Wang. Identification of a COL1A2 Mutation with a Deletion Spanning Coding and Intronic Sequence in Exon 19 and Intron 19 in a Fetus with Osteogenesis Imperfecta Type II. Elsevier, 2012.

MLA (9th ed.) Citation

Chih-Ping Chen, et al. Identification of a COL1A2 Mutation with a Deletion Spanning Coding and Intronic Sequence in Exon 19 and Intron 19 in a Fetus with Osteogenesis Imperfecta Type II. Elsevier, 2012.